Canonical Allele Identifier: CA497768523

Gene: AURKB

Linked Data

• gnomAD v4: 17-8204874-G-T
• MyVariant Identifiers: chr17:g.8108192G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8204874G>T , CM000679.2:g.8204874G>T	GRCh38
NC_000017.10:g.8108192G>T , CM000679.1:g.8108192G>T	GRCh37
NC_000017.9:g.8048917G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585124.6:c.1032C>A MANE Select	ENSP00000463999.1:p.Ala344=
ENST00000316199.10:c.1035C>A	ENSP00000313950.6:p.Ala345=
ENST00000534871.5:c.909C>A	ENSP00000443869.1:p.Ala303=
ENST00000578549.5:c.936C>A	ENSP00000462207.1:p.Ala312=
ENST00000584972.5:c.724C>A
ENST00000585124.5:c.1032C>A	ENSP00000463999.1:p.Ala344=
NM_001256834.1:c.909C>A	NP_001243763.1:p.Ala303=
NM_001256834.2:c.909C>A	NP_001243763.1:p.Ala303=
NM_001284526.1:c.1035C>A	NP_001271455.1:p.Ala345=
NM_001313950.1:c.1032C>A	NP_001300879.1:p.Ala344=
NM_001313951.1:c.909C>A	NP_001300880.1:p.Ala303=
NM_001313952.1:c.912C>A	NP_001300881.1:p.Ala304=
NM_001313953.1:c.936C>A	NP_001300882.1:p.Ala312=
NM_001313954.1:c.576C>A	NP_001300883.1:p.Ala192=
NM_001313955.1:c.528C>A	NP_001300884.1:p.Ala176=
NM_004217.3:c.1032C>A	NP_004208.2:p.Ala344=
NR_132730.1:n.1012C>A
NR_132731.1:n.897C>A
XM_011524070.1:c.936C>A	XP_011522372.1:p.Ala312=
XM_011524072.1:c.909C>A	XP_011522374.1:p.Ala303=
XR_934118.1:n.1241C>A
NM_001313953.2:c.936C>A	NP_001300882.1:p.Ala312=
XM_011524072.3:c.909C>A	XP_011522374.1:p.Ala303=
XM_017025307.2:c.909C>A	XP_016880796.1:p.Ala303=
XM_017025308.2:c.813C>A	XP_016880797.1:p.Ala271=
XM_017025309.1:c.576C>A	XP_016880798.1:p.Ala192=
XM_017025310.1:c.576C>A	XP_016880799.1:p.Ala192=
XM_017025311.1:c.576C>A	XP_016880800.1:p.Ala192=
NM_004217.4:c.1032C>A MANE Select	NP_004208.2:p.Ala344=
NM_001256834.3:c.909C>A	NP_001243763.1:p.Ala303=
NM_001284526.2:c.1035C>A	NP_001271455.1:p.Ala345=
NM_001313950.2:c.1032C>A	NP_001300879.1:p.Ala344=
NM_001313952.2:c.912C>A	NP_001300881.1:p.Ala304=
NM_001313953.3:c.936C>A	NP_001300882.1:p.Ala312=
NM_001313954.2:c.576C>A	NP_001300883.1:p.Ala192=
NM_001313955.2:c.528C>A	NP_001300884.1:p.Ala176=
NR_132730.2:n.961C>A